Canonical Allele Identifier: CA393893714

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93521495G>C (hg19) ; chr15:g.92978265G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978265G>C , CM000677.2:g.92978265G>C	GRCh38
NC_000015.9:g.93521495G>C , CM000677.1:g.93521495G>C	GRCh37
NC_000015.8:g.91322499G>C	NCBI36
NG_012826.1:g.82945G>C
NG_012826.2:g.82945G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2116G>C
ENST00000628118.2:c.1643G>C
ENST00000700551.1:c.*1440G>C	ENSP00000515057.1:n.*1440G>C
ENST00000394196.9:c.2609G>C MANE Select	ENSP00000377747.4:p.Gly870Ala
ENST00000635856.1:n.3181G>C
ENST00000636306.1:n.169G>C
ENST00000636881.1:c.1980G>C
ENST00000637572.1:n.3353G>C
ENST00000394196.8:c.2609G>C	ENSP00000377747.4:p.Gly870Ala
ENST00000625463.1:c.149G>C	ENSP00000486391.1:p.Gly50Ala
ENST00000626874.2:c.2609G>C	ENSP00000486629.1:p.Gly870Ala
ENST00000628118.1:n.388G>C
NM_001271.3:c.2609G>C	NP_001262.3:p.Gly870Ala
NM_001271.4:c.2609G>C MANE Select	NP_001262.3:p.Gly870Ala